Epstein-Barr virus (EBV) is a ubiquitous herpes virus recognized as the cause of infectious mononucleosis, and a variety of human neoplasia including nasopharyngeal carcinoma, thymic carcinoma, and lymphoma. This virus is capable of establishing latency in B- lymphocytes and epithelial cells. It is a potent polyclonal B cell activator, and incites an intense T-cell mediated immune response. EBV has recently been associated with several ocular inflammatory disorders including aqueous tear deficiency, keratitis, uveitis, and retinitis. With the exception of demonstrating EBV antigens in the lacrimal glands of tear deficient patients, the causal relationship of EBV to these ocular inflammatory diseases has been based on serologic evidence of acute or chronic infection. Unlike other herpes viruses which cause disease by viral replication, EBV is most often found in a latent, non-replicative state. Diagnosis of infection is based on demonstrating viral genomes. Conventional techniques such as in-situ hybridization of Southern blot analysis lack sufficient sensitivity to detect DNA in minute specimens, such as those obtained from the eye and adnexae. A novel method of DNA amplification, polymerase chain reaction (PCR), has recently been introduced. PCR can specifically amplify viral genome up to 1 x 107 times in several hours. PCR has been utilized to detect Papilloma virus and HIV infections. The principal investigator plans to apply the PCR to detect EBV DNA within ocular tissue and fluid. The initial phase of this project will involve refining the technique to detect DNA in EBV- infected lymphoblastoid cells. Following the establishment of positive controls, fresh human autopsy tissue including conjunctiva, cornea, uvea, retina, and lacrimal gland will be surveyed for the presence of DNA. PCR will also be used to examine paraffin embedded pathology specimens. This work is essential to establish the efficacy of PCR as a diagnostic tool for future clinical and laboratory investigation of EBV as an inciting factor for ocular inflammation.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Small Research Grants (R03)
Project #
1R03EY008193-01
Application #
3426508
Study Section
Vision Research and Training Committee (VSN)
Project Start
1989-03-01
Project End
1990-02-28
Budget Start
1989-03-01
Budget End
1990-02-28
Support Year
1
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Miami School of Medicine
Department
Type
Schools of Medicine
DUNS #
City
Miami
State
FL
Country
United States
Zip Code
33101
Fox, G M; Crouse, C A; Chuang, E L et al. (1991) Detection of herpesvirus DNA in vitreous and aqueous specimens by the polymerase chain reaction. Arch Ophthalmol 109:266-71
Levine, J; Pflugfelder, S C; Yen, M et al. (1990) Detection of the complement (CD21)/Epstein-Barr virus receptor in human lacrimal gland and ocular surface epithelia. Reg Immunol 3:164-70
Pflugfelder, S C; Crouse, C; Pereira, I et al. (1990) Amplification of Epstein-Barr virus genomic sequences in blood cells, lacrimal glands, and tears from primary Sjogren's syndrome patients. Ophthalmology 97:976-84
McLeish, W; Pflugfelder, S C; Crouse, C et al. (1990) Interferon treatment of herpetic keratitis in a patient with acquired immunodeficiency syndrome. Am J Ophthalmol 109:93-5
Crouse, C A; Pflugfelder, S C; Pereira, I et al. (1990) Detection of herpes viral genomes in normal and diseased corneal epithelium. Curr Eye Res 9:569-81
Crouse, C A; Pflugfelder, S C; Cleary, T et al. (1990) Detection of Epstein-Barr virus genomes in normal human lacrimal glands. J Clin Microbiol 28:1026-32